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Q30485962-44156688-D6E9-44AA-A522-EF186457A504
Q30485962-44156688-D6E9-44AA-A522-EF186457A504
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30485962-44156688-D6E9-44AA-A522-EF186457A504
Connexin32 mutations cause loss of function in Schwann cells and oligodendrocytes leading to PNS and CNS myelination defects
P2860
Q30485962-44156688-D6E9-44AA-A522-EF186457A504
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30485962-44156688-D6E9-44AA-A522-EF186457A504
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wasDerivedFrom
0ad0f164a321b49b7729cfbd4adfd8829984f81b
P2860
Molecular interaction of connexin 30.3 and connexin 31 suggests a dominant-negative mechanism associated with erythrokeratodermia variabilis